ClinVar Miner

List of variants in gene NLRP12 studied for not specified

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Total variants: 27
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HGVS dbSNP gnomAD frequency
NM_144687.4(NLRP12):c.371-43C>T rs6509827 0.95894
NM_144687.4(NLRP12):c.2394G>A (p.Gln798=) rs4806773 0.85135
NM_144687.4(NLRP12):c.-140T>A rs4419163 0.78722
NM_144687.4(NLRP12):c.3098+99G>A rs2042296 0.54490
NM_144687.4(NLRP12):c.2072+45G>C rs58572468 0.51324
NM_144687.4(NLRP12):c.-12C>T rs4539722 0.44990
NM_144687.4(NLRP12):c.116G>T (p.Gly39Val) rs34436714 0.22387
NM_144687.4(NLRP12):c.1206C>G (p.Phe402Leu) rs34971363 0.05162
NM_144687.4(NLRP12):c.289+18C>T rs116129563 0.03610
NM_144687.4(NLRP12):c.969T>G (p.Leu323=) rs142063194 0.00814
NM_144687.4(NLRP12):c.956C>G (p.Pro319Arg) rs35401786 0.00803
NM_144687.4(NLRP12):c.424G>A (p.Asp142Asn) rs34330210 0.00799
NM_144687.4(NLRP12):c.910C>T (p.His304Tyr) rs141245482 0.00392
NM_144687.4(NLRP12):c.2701G>C (p.Val901Leu) rs104895568 0.00265
NM_144687.4(NLRP12):c.1462G>T (p.Gly488Trp)
NM_144687.4(NLRP12):c.1884G>T (p.Gln628His)
NM_144687.4(NLRP12):c.2046A>G (p.Ala682=) rs886054608
NM_144687.4(NLRP12):c.2072+2_2072+3insTT rs104895565
NM_144687.4(NLRP12):c.2073-42C>G rs2866112
NM_144687.4(NLRP12):c.2244-73_2244-72dup rs34166148
NM_144687.4(NLRP12):c.2244-85dup rs34166148
NM_144687.4(NLRP12):c.2469C>A (p.Leu823=) rs12460528
NM_144687.4(NLRP12):c.2469C>T (p.Leu823=) rs12460528
NM_144687.4(NLRP12):c.2830C>T (p.Arg944Trp) rs104895570
NM_144687.4(NLRP12):c.2927+4_2927+5dup rs763190690
NM_144687.4(NLRP12):c.46dup (p.Tyr16fs) rs1599879570
NM_144687.4(NLRP12):c.838C>T (p.Gln280Ter) rs145049569

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